דרושים נאנובל בע"מ

1. Quality system Compliance: Ensure compliance with global regulatory requirements and standards for medical devices, including FDA QSR, ISO 13485, EU MDR, and others as applicable.
2. Design Control & Risk Management: Participate in design control activities, ensuring quality considerations are integrated into product development processes. Lead risk management activities (FMEA, risk analysis) to identify and mitigate potential issues.
3. Process Validation and Verification: Oversee the validation and verification of design and manufacturing processes. Ensure robust testing methodologies are applied to prove that designs meet all requirements and regulations.
4. Documentation and Records: Write and Maintain comprehensive documentation that meets regulatory and company requirements throughout the product development lifecycle. Ensure traceability and accessibility

If you are looking for a challenging position, collaborated multi-disciplinary software development and on-site action in a rapidly changing and evolving market JOIN US!

Do you want to join an international team within an innovative fast-paced medical device company? Grab the opportunity and make good use of your Mathematical and programming skills and affinity to medical device